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A pilot study of single nucleotide polymorphisms in the interleukin‐6 receptor and their effects on pre‐ and post‐transplant serum mediator level and outcome after allogeneic stem cell transplantation

Clinical and experimental immunology, 2018-07, Vol.193 (1), p.130-141

2018

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Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

Journal of medical genetics, 2007-10, Vol.44 (10), p.615-620

2007

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Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients

Leukemia, 2013-07, Vol.27 (7), p.1520-1526

2013

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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13

Nature genetics, 2001-08, Vol.28 (4), p.365-370

2001

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Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

Journal of medical genetics, 2002-10, Vol.39 (10), p.722-733

2002

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Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia

Leukemia, 2017-05, Vol.31 (5), p.1108-1116

2017

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The CD34+ Cell Dose Matters in Hematopoietic Stem Cell Transplantation with Peripheral Blood Stem Cells from Sibling Donors

Clinical hematology international, 2020, Vol.2 (2), p.74-81

2020

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Safety and efficacy of the combination of pegylated interferon- alpha 2b and dasatinib in newly diagnosed chronic-phase chronic myeloid leukemia patients

Leukemia, 2016-09, Vol.30 (9), p.1853-1860

2016

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Safety and efficacy of the combination of pegylated interferon-α2b and dasatinib in newly diagnosed chronic-phase chronic myeloid leukemia patients

Leukemia, 2016-09, Vol.30 (9), p.1853-1860

2016

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Selecting and deselecting imatinib-resistant clones: observations made by longitudinal, quantitative monitoring of mutated BCR-ABL

Leukemia, 2005-12, Vol.19 (12), p.2159-2165

2005

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Treatment outcome in adults with acute lymphoblastic leukemia: 50% long-term disease-free survival

Leukemia, 2007-10, Vol.21 (10), p.2203-2204

2007

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A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association

Journal of human genetics, 2006-10, Vol.51 (10), p.864-871

2006

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Activated prothrombin complex concentrate (FEIBA®) treatment during surgery in patients with inhibitors to FVIII/IX

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-03, Vol.10 (2), p.174-178

2004

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Addition of Anti-thymocyte Globulin in Allogeneic Stem Cell Transplantation With Peripheral Stem Cells From Matched Unrelated Donors Improves Graft-Versus-Host Disease and Relapse Free Survival

Clinical lymphoma, myeloma and leukemia, 2021-09, Vol.21 (9), p.598-605

2021

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EBMT prospective observational study on allogeneic hematopoietic stem cell transplantation in T-prolymphocytic leukemia (T-PLL)

Bone marrow transplantation (Basingstoke), 2019-09, Vol.54 (9), p.1391-1398

2019

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The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9079-9084

1996

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Allogeneic haematopoietic stem cell transplant in patients with lower risk myelodysplastic syndrome: a retrospective analysis on behalf of the Chronic Malignancy Working Party of the EBMT

Bone marrow transplantation (Basingstoke), 2017-02, Vol.52 (2), p.209-215

2017

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HLA-DPB1 mismatch reduce relapse and improve survival in T-cell replete unrelated donor allogeneic stem cell transplantation

Bone marrow transplantation (Basingstoke), 2020-08, Vol.55 (8), p.1658-1661

2020

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Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3–34.13

Journal of medical genetics, 2004-03, Vol.41 (3), p.208-212

2004

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Allogeneic haematopoietic stem cell transplant in patients with lower risk myelodysplastic syndrome: a retrospective analysis on behalf of the Chronic Malignancy Working Party of the EBMT

Bone marrow transplantation (Basingstoke), 2017-07, Vol.52 (7), p.1081-1081

2017

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Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression

Acta dermato-venereologica, 2001-06, Vol.81 (3), p.163-170

2001

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A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations

Journal of investigative dermatology, 2002-01, Vol.118 (1), p.87-93

2002

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Immunohistochemical and Mutation Analyses Demonstrate That Procollagen VII Is Processed to Collagen VII through Removal of the NC-2 Domain

The Journal of cell biology, 1995-10, Vol.131 (2), p.551-559

1995

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A pilot study of single nucleotide polymorphisms in the interleukin‐6 receptor and their effects on pre‐ and post‐transplant serum mediator level and outcome after allogeneic stem cell transplantation

Congenital ichthyosis: mutations in ichthyin are associated with specific structural abnormalities in the granular layer of epidermis

Impact of malignant stem cell burden on therapy outcome in newly diagnosed chronic myeloid leukemia patients

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13

Genotype-phenotype relationships in Berardinelli-Seip congenital lipodystrophy

S238: MATCHED RELATED VERSUS UNRELATED VERSUS HAPLOIDENTICAL DONORS FOR ALLOGENEIC TRANSPLANTATION IN AML PATIENTS ACHIEVING FIRST COMPLETE REMISSION AFTER TWO INDUCTION COURSES: A STUDY FROM THE ALWP/EBMT

Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia

Bortezomib consolidation after autologous stem cell transplantation in multiple myeloma: a Nordic Myeloma Study Group randomized phase 3 trial

The CD34+ Cell Dose Matters in Hematopoietic Stem Cell Transplantation with Peripheral Blood Stem Cells from Sibling Donors

Safety and efficacy of the combination of pegylated interferon- alpha 2b and dasatinib in newly diagnosed chronic-phase chronic myeloid leukemia patients

Safety and efficacy of the combination of pegylated interferon-α2b and dasatinib in newly diagnosed chronic-phase chronic myeloid leukemia patients

Selecting and deselecting imatinib-resistant clones: observations made by longitudinal, quantitative monitoring of mutated BCR-ABL

Treatment outcome in adults with acute lymphoblastic leukemia: 50% long-term disease-free survival

A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association

Activated prothrombin complex concentrate (FEIBA®) treatment during surgery in patients with inhibitors to FVIII/IX

Addition of Anti-thymocyte Globulin in Allogeneic Stem Cell Transplantation With Peripheral Stem Cells From Matched Unrelated Donors Improves Graft-Versus-Host Disease and Relapse Free Survival

EBMT prospective observational study on allogeneic hematopoietic stem cell transplantation in T-prolymphocytic leukemia (T-PLL)

The Genetic Basis of Epidermolysis Bullosa Simplex with Mottled Pigmentation

Allogeneic haematopoietic stem cell transplant in patients with lower risk myelodysplastic syndrome: a retrospective analysis on behalf of the Chronic Malignancy Working Party of the EBMT

HLA-DPB1 mismatch reduce relapse and improve survival in T-cell replete unrelated donor allogeneic stem cell transplantation

Assignment of the locus for ichthyosis prematurity syndrome to chromosome 9q33.3–34.13

Allogeneic haematopoietic stem cell transplant in patients with lower risk myelodysplastic syndrome: a retrospective analysis on behalf of the Chronic Malignancy Working Party of the EBMT

Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression

A Site-Specific Plectin Mutation Causes Dominant Epidermolysis Bullosa Simplex Ogna: Two Identical De Novo Mutations

Immunohistochemical and Mutation Analyses Demonstrate That Procollagen VII Is Processed to Collagen VII through Removal of the NC-2 Domain

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